A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18196359



Internal ID20763399
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:46364201..46387400hg38UCSC Ensembl
chr12:46757984..46781183hg19UCSC Ensembl
Cytoband12q13.11
Allele length
AssemblyAllele length
hg3823200
hg1923200
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6457701
Supporting Variants
Samples
Known GenesSLC38A2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18196359
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00038


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